Steric, Electronic, and Secondary Effects on the Coordination Chemistry of Ionic Phosphine Ligands and the Catalytic Behavior of Their Metal Complexes

被引:62
|
作者
Snelders, Dennis J. M. [1 ]
van Koten, Gerard [1 ]
Gebbink, Robertus J. M. Klein [1 ]
机构
[1] Univ Utrecht, Debye Inst Nanomat Sci, Fac Sci, NL-3584 CH Utrecht, Netherlands
关键词
homogeneous catalysis; noncovalent interactions; P ligands; supramolecular chemistry; transition metals; WATER-SOLUBLE PHOSPHINES; NUCLEAR-MAGNETIC-RESONANCE; HEXACATIONIC DENDRIPHOS LIGANDS; STABILIZED PHOSPHENIUM ADDUCTS; CROSS-COUPLING REACTION; RAY CRYSTAL-STRUCTURE; ORGANOMETALLIC CHEMISTRY; PHOSPHORUS LIGANDS; AQUEOUS-PHASE; HOMOGENEOUS CATALYSIS;
D O I
10.1002/chem.201002508
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The effects of introducing ionic functionalities in phosphine ligands on the coordination chemistry of these ligands and the catalytic behavior of the corresponding metal complexes are reviewed. The steric and electronic consequences of such functionalizations are discussed. Apart from these steric and electronic effects, the presence of charged groups often leads to additional, supramolecular interactions that occur in the second coordination sphere of the metal complex, such as intramolecular, interligand hydrogen bonding and Coulombic repulsion. These interactions can significantly alter the behavior of the phosphine ligand in question. Such effects have been observed in phosphine metal association/dissociation equilibria, ligand substitution reactions, and stereoisomerism in phosphine-metal complexes. By drawing general conclusions, this review offers an insight into the coordination and catalytic behavior of phosphine ligands containing ionic functionalities and their corresponding metal complexes.
引用
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页码:42 / 57
页数:16
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